A Review of the Most Important Natural Antioxidants and Effective Medicinal Plants in Traditional Medicine on Prostate Cancer and Its Disorders
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TRP Channels in Visceral Pain
Send Orders of Reprints at [email protected] 23 The Open Pain Journal, 2013, 6, (Suppl 1: M4) 23-30 Open Access TRP Channels in Visceral Pain L. Ashley Blackshaw*,1,2, Stuart M. Brierley2, Andrea M. Harrington2 and Patrick A. Hughes2 1Wingate Institute for Neurogastroenterology, Centre for Digestive Diseases, Institute of Cell and Molecular Science, Barts and The London School of Medicine and Dentistry, Queen Mary University of London; 2Nerve-Gut Research Laboratory, Discipline of Medicine, The University of Adelaide, Adelaide, South Australia, Australia 5000. Abstract: Visceral pain is both different and similar to somatic pain - different in being poorly localized and usually referred elsewhere to the body wall, but similar in many of the molecular mechanisms it employs (like TRP channels) and the specialization of afferent endings to detect painful stimuli. TRPV1 is sensitive to low pH. pH is lowest in gastric juice, which may cause severe pain when exposed to the oesophageal mucosa, and probably works via TRPV1. TRPV1 is found in afferent fibres throughout the viscera, and the TRPV1 agonist capsaicin can recapitulate symptoms experienced in disease. TRPV1 is also involved in normal mechanosensory function in the gut. Roles for TRPV4 and TRPA1 have also been described in visceral afferents, and TRPV4 is highly enriched in them, where it plays a major role in both mechanonociception and chemonociception. It may provide a visceral-specific nociceptor target for drug development. TRPA1 is also involved in mechano-and chemosensory function, but not as selectively as TRPV4. TRPA1 is colocalized with TRPV1 in visceral afferents, where they influence each other’s function. -
Toxic Effects As a Result of Herbal Medicine Intake Toxic Effects As a Result of Herbal Medicine Intake
ProvisionalChapter chapter 9 Toxic Effects as a Result of Herbal Medicine Intake Toxic Effects as a Result of Herbal Medicine Intake Nudrat Fatima and Naira Nayeem Nudrat Fatima and Naira Nayeem Additional information is available at the end of the chapter Additional information is available at the end of the chapter http://dx.doi.org/10.5772/64468 Abstract Concurrent use of herbs with therapeutic drugs increases the potential of herb-drug interactions. The clinical importance of herb-drug interactions is associated with the particular herb, drug, and patient profile. Herbs are potentially potent as they affect body functions. The use herbal medicine and supplements can be risky as they are not subject to review by the FDA. In this chapter, we make an attempt to discuss the possible reasons for toxic effects, types of toxicities, some reported cases of toxicities involving the use of herbal medicine alone, and some herb-drug interactions. In addition to this, possible ways to reduce toxic effects of herbal medicines have also been discussed. Keywords: herbal medicine, toxicity, reported cases, herb-drug interaction 1. Introduction Herbal medicines are advertised to be free from side effects, which is a myth. A large number of people still rely on herbal medicines, and some people take herbal medicines along with routine allopathic medicines especially in cases of diabetes, hypertension, thyroid disease, etc., where the patient is on long-term or lifelong treatment. Many commercial websites are available on Internet, which insist that herbal medicines have no side effects. In underdeveloped and developing countries, there are no specific laws for herbal practitioners and companies marketing herbal products. -
Functional P53 Is Required for Triptolide-Induced Apoptosis and AP-1 and Nuclear Factor-Κb Activation in Gastric Cancer Cells
Oncogene (2001) 20, 8009 ± 8018 ã 2001 Nature Publishing Group All rights reserved 0950 ± 9232/01 $15.00 www.nature.com/onc Functional p53 is required for triptolide-induced apoptosis and AP-1 and nuclear factor-kB activation in gastric cancer cells Xiao-Hua Jiang1,2,5, Benjamin Chun-Yu Wong*,2,5, Marie Chia-Mi Lin3, Geng-Hui Zhu2, Hsiang-Fu Kung3, Shi-Hu Jiang1, Dan Yang4 and Shiu-Kum Lam2 1Department of Gastroenterology, Rui-jin Hospital, Shanghai, Peoples Republic of China; 2Department of Medicine, University of Hong Kong, Hong Kong; 3Institute of Molecular Biology, University of Hong Kong, Hong Kong; 4Department of Chemistry, University of Hong Kong, Hong Kong Triptolide, a major component in the extract of Chinese Introduction herbal plant Tripterygium wilfordii Hook f (TWHf), has potential anti-neoplastic eect. In the present study we Tripterygium wilfordii Hook f (TWHf) has been used investigated the potential therapeutic eects and mechan- in traditional Chinese medicine for centuries. Its crude isms of triptolide against human gastric cancer cells. extracts continue to be used to treat a variety of Four gastric cancer cell lines with dierent p53 status, autoimmune diseases, such as rheumatoid arthritis, AGS and MKN-45 (wild type p53); MKN-28 and SGC- nephritis, and systemic lupus erythematosus (Qin et al., 7901 (mutant p53) were observed as to cell growth 1981; Tao et al., 1989; Jiang et al., 1994). It has been inhibition and induction of apoptosis in response to suggested that the major therapeutic eects of TWHf triptolide treatment. We showed that triptolide inhibited are from ingredients such as triptolide, tripdiolide, cell growth, induced apoptosis and suppressed NK-kB triptonide, and triptophenolide (Zhang et al., 1990). -
Diterpenoids As Potential Anti-Malarial Compounds from Andrographis Paniculata Manish Kumar Dwivedi, Shringika Mishra, Shruti Sonter and Prashant Kumar Singh*
Dwivedi et al. Beni-Suef University Journal of Basic and Applied Sciences Beni-Suef University Journal of (2021) 10:7 https://doi.org/10.1186/s43088-021-00098-8 Basic and Applied Sciences RESEARCH Open Access Diterpenoids as potential anti-malarial compounds from Andrographis paniculata Manish Kumar Dwivedi, Shringika Mishra, Shruti Sonter and Prashant Kumar Singh* Abstract Background: The objectives of the current study are to evaluate the traditionally used medicinal plants Andrographis paniculata for in vitro anti-malarial activity against human malarial parasite Plasmodium falciparum and to further characterize the anti-malarial active extract of A. paniculata using spectroscopic and chromatographic methods. Results: The chloroform extract of A. paniculata displayed anti-malarial activity with IC50 values 6.36 μg/ml against 3D7 strain and 5.24 μg/ml against K1 strains respectively with no evidence of significant cytotoxicity against mammalian cell line (CC50 > 100 μg/ml). LC-MS analysis of the extract led to the identification of 59 compounds based on their chromatographic and mass spectrometric features (a total of 35 compounds are present in positive ion and 24 compounds in negative ion mode). We have identified 5 flavonoids and 30 compounds as diterpenoids in positive ion mode, while in the negative mode all identified compounds were diterpenoids. Characterization of the most promising class of compound diterpenoids using HPLC-LC-ESI-MS/MS was also undertaken. Conclusions: The in vitro results undoubtedly validate the traditional use of A. paniculata for the treatment of malaria. The results have led to the identification of diterpenoids from IGNTU_06 extract as potential anti-malarial compounds that need to be further purified and analyzed in anti-malarial drug development programs. -
Note: the Letters 'F' and 'T' Following the Locators Refers to Figures and Tables
Index Note: The letters ‘f’ and ‘t’ following the locators refers to figures and tables cited in the text. A Acyl-lipid desaturas, 455 AA, see Arachidonic acid (AA) Adenophostin A, 71, 72t aa, see Amino acid (aa) Adenosine 5-diphosphoribose, 65, 789 AACOCF3, see Arachidonyl trifluoromethyl Adlea, 651 ketone (AACOCF3) ADP, 4t, 10, 155, 597, 598f, 599, 602, 669, α1A-adrenoceptor antagonist prazosin, 711t, 814–815, 890 553 ADPKD, see Autosomal dominant polycystic aa 723–928 fragment, 19 kidney disease (ADPKD) aa 839–873 fragment, 17, 19 ADPKD-causing mutations Aβ, see Amyloid β-peptide (Aβ) PKD1 ABC protein, see ATP-binding cassette protein L4224P, 17 (ABC transporter) R4227X, 17 Abeele, F. V., 715 TRPP2 Abbott Laboratories, 645 E837X, 17 ACA, see N-(p-amylcinnamoyl)anthranilic R742X, 17 acid (ACA) R807X, 17 Acetaldehyde, 68t, 69 R872X, 17 Acetic acid-induced nociceptive response, ADPR, see ADP-ribose (ADPR) 50 ADP-ribose (ADPR), 99, 112–113, 113f, Acetylcholine-secreting sympathetic neuron, 380–382, 464, 534–536, 535f, 179 537f, 538, 711t, 712–713, Acetylsalicylic acid, 49t, 55 717, 770, 784, 789, 816–820, Acrolein, 67t, 69, 867, 971–972 885 Acrosome reaction, 125, 130, 301, 325, β-Adrenergic agonists, 740 578, 881–882, 885, 888–889, α2 Adrenoreceptor, 49t, 55, 188 891–895 Adult polycystic kidney disease (ADPKD), Actinopterigy, 223 1023 Activation gate, 485–486 Aframomum daniellii (aframodial), 46t, 52 Leu681, amino acid residue, 485–486 Aframomum melegueta (Melegueta pepper), Tyr671, ion pathway, 486 45t, 51, 70 Acute myeloid leukaemia and myelodysplastic Agelenopsis aperta (American funnel web syndrome (AML/MDS), 949 spider), 48t, 54 Acylated phloroglucinol hyperforin, 71 Agonist-dependent vasorelaxation, 378 Acylation, 96 Ahern, G. -
An in Silico Study of the Ligand Binding to Human Cytochrome P450 2D6
AN IN SILICO STUDY OF THE LIGAND BINDING TO HUMAN CYTOCHROME P450 2D6 Sui-Lin Mo (Doctor of Philosophy) Discipline of Chinese Medicine School of Health Sciences RMIT University, Victoria, Australia January 2011 i Declaration I hereby declare that this submission is my own work and to the best of my knowledge it contains no materials previously published or written by another person, or substantial proportions of material which have been accepted for the award of any other degree or diploma at RMIT university or any other educational institution, except where due acknowledgment is made in the thesis. Any contribution made to the research by others, with whom I have worked at RMIT university or elsewhere, is explicitly acknowledged in the thesis. I also declare that the intellectual content of this thesis is the product of my own work, except to the extent that assistance from others in the project‘s design and conception or in style, presentation and linguistic expression is acknowledged. PhD Candidate: Sui-Lin Mo Date: January 2011 ii Acknowledgements I would like to take this opportunity to express my gratitude to my supervisor, Professor Shu-Feng Zhou, for his excellent supervision. I thank him for his kindness, encouragement, patience, enthusiasm, ideas, and comments and for the opportunity that he has given me. I thank my co-supervisor, A/Prof. Chun-Guang Li, for his valuable support, suggestions, comments, which have contributed towards the success of this thesis. I express my great respect to Prof. Min Huang, Dean of School of Pharmaceutical Sciences at Sun Yat-sen University in P.R.China, for his valuable support. -
Recent Applications of HSCCC/HPCPC to Natural Product Isolation from Medicinal Plants and Algae
1 Table S2 (complete version of Table 12). Recent applications of HSCCC/HPCPC to natural product isolation from medicinal plants and algae Compounds Matrix a Solvent systems (volume ratio) b Mode c MP d Ref. e Flavonoids Flavonoids Ampelopsis grossedentata, leaf Hex–EtOAc–MeOH–water (1:6:1.5:7.5) LP 249 Flavonoids Byrsonima crassa, leaf EtOAc–PrOH–water (14:0.8:8) UP 250 Anthocyanins (sambubiosides) Vaccinium myrtillus, fruit MtBE–BuOH–CH3CN–water–TFA LP 251 (1:4:1:5:0.01) Flavonoids Patrinia villosa Hex–EtOAc–MeOH–water (10:11:11:8) LP 252 Catechin, stilbene derivative Rheum tanguticum, root and rhizome EtOAc–EtOH–water (25:1:25) → (5:1:5) stepwise LP 253 Catechin constituents Camellia sinensis cultivars, leaf Hex–EtOAc–MeOH–water (1:6:1:6), (1:7:1:7), LP 254 (1:5:1:5), (1:6.5:1:6.5) Flavonoids Paeonia suffruticosa, flower EtOAc–EtOH–AcOH–water (4:1:0.25:5) LP 255 Baicalein, wogonin, oroxylin Scutellaria baicalensis, root Hex–EtOAc–BuOH–water (1:1:8:10) stepwise LP 256 A Baicalin, wogonoside Scutellaria baicalensis, root EtOAc–MeOH–1% AcOH (5:0.5:5) LP 257 Flavonoid glycosides Trollius ledebouri, herb EtOAc–BuOH–water (2:1:3) LP 183 Flavonoid glycosides Epimedium koreamum, herb CHCl3–MeOH–water (4:3.5:2) LP 258 C-glycosylflavones Patrinia villosa EtOAC–BuOH-water (2:1:3) LP 259 Flavanone glucoside Carthamus tinctorum, flower EtOAc–MeOH–water (5:1:5) [silica step clean- LP 260 up before HSCCC] Flavonoids Salix alba, bark Hex–EtOAc–MeOH–water (2:2:2:3) LP 261 Flavonoids Oroxylum indicum, seed Hex–EtOAc–MeOH–water (1:1.2:1:1), (1:2:1:1), -
Health Benefits of Herbs and Spices How New Findings Will Disrupt Global Spice Industry?
Health Benefits of Herbs and Spices How new findings will disrupt global spice industry? Bharat B. Aggarwal, Ph.D. Inflammation Research Center, San Diego, California; USA Retired Professor & Chief, Cytokine Research, Department of Experimental Therapeutics, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas Former Senior Scientist, Genentech Inc., South San Francisco, California PDF, University of California, San Francisco; Ph.D., University of California, Berkeley Hosted by Gerhard Weber & Anders Mattsson ESA (European Spice Association) esa-spices.org May 31st- June 1st, 2017, Annual Meeting General Assembly, Bordeaux, France. Talk: Wednesday, May 31st, 2017: 4:00 to 5:00 PM Goa: Land of Vasco de Gama http://www.isncd.com Cochin: The Land of Spices Healing with Spices Julie Chugh Global Cancer Incidence Foods to Fight Cancer Denis Gingras, Richard Béliveau: 2005 Cancer incidence is less in spice consuming countries 183 Comparison of Cancer Incidence in USA and India Cancer USA India Cases Deaths Cases Deaths Breast 660 160 79 41 Prostate 690 130 20 9 Colon/Rectum 530 220 30 18 Lung 660 580 38 37 Head & Neck SCC 140 44 153 103 Liver 41 44 12 13 Pancreas 108 103 8 8 Stomach 81 50 33 30 Melanoma 145 27 1.8 1 Testis 21 1 3 1 Bladder 202 43 15 11 Kidney 115 44 6 4 Brain, Nervous system 65 47 19 14 Thyroid 55 5 12 3 Endometrial Cancers 163 41 132 72 Ovary 76 50 20 2 Multiple myeloma 50 40 6 5 Leukemia 100 70 19 17 Non-Hodgkin lymphoma 180 90 17 15 Hodgkin's disease 20 5 7 4 Showing cases per 1 million persons calculated on the basis of current consensus: Endometrial cancers include Cervix uteri and Corpus uteri. -
Cochrane Library
Cochrane Library Cochrane Database of Systematic Reviews Herbal therapy for treating rheumatoid arthritis (Review) Cameron M, Gagnier JJ, Chrubasik S Cameron M, Gagnier JJ, Chrubasik S. Herbal therapy for treating rheumatoid arthritis. Cochrane Database of Systematic Reviews 2011, Issue 2. Art. No.: CD002948. DOI: 10.1002/14651858.CD002948.pub2. www.cochranelibrary.com Herbal therapy for treating rheumatoid arthritis (Review) Copyright © 2011 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd. Cochrane Trusted evidence. Informed decisions. Library Better health. Cochrane Database of Systematic Reviews T A B L E O F C O N T E N T S HEADER......................................................................................................................................................................................................... 1 ABSTRACT..................................................................................................................................................................................................... 1 PLAIN LANGUAGE SUMMARY....................................................................................................................................................................... 2 SUMMARY OF FINDINGS.............................................................................................................................................................................. 3 BACKGROUND............................................................................................................................................................................................. -
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STRUCTURAL AND FUNCTIONAL STUDIES OF TRPML1 AND TRPP2 Nicole Marie Benvin Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Graduate School of Arts and Sciences COLUMBIA UNIVERSITY 2017 © 2017 Nicole Marie Benvin All Rights Reserved ABSTRACT Structural and Functional Studies of TRPML1 and TRPP2 Nicole Marie Benvin In recent years, the determination of several high-resolution structures of transient receptor potential (TRP) channels has led to significant progress within this field. The primary focus of this dissertation is to elucidate the structural characterization of TRPML1 and TRPP2. Mutations in TRPML1 cause mucolipidosis type IV (MLIV), a rare neurodegenerative lysosomal storage disorder. We determined the first high-resolution crystal structures of the human TRPML1 I-II linker domain using X-ray crystallography at pH 4.5, pH 6.0, and pH 7.5. These structures revealed a tetramer with a highly electronegative central pore which plays a role in the dual Ca2+/pH regulation of TRPML1. Notably, these physiologically relevant structures of the I-II linker domain harbor three MLIV-causing mutations. Our findings suggest that these pathogenic mutations destabilize not only the tetrameric structure of the I-II linker, but also the overall architecture of full-length TRPML1. In addition, TRPML1 proteins containing MLIV- causing mutations mislocalized in the cell when imaged by confocal fluorescence microscopy. Mutations in TRPP2 cause autosomal dominant polycystic kidney disease (ADPKD). Since novel technological advances in single-particle cryo-electron microscopy have now enabled the determination of high-resolution membrane protein structures, we set out to solve the structure of TRPP2 using this technique. -
WO 2007/095718 Al
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date PCT (10) International Publication Number 30 August 2007 (30.08.2007) WO 2007/095718 Al (51) International Patent Classification: 5S2 (CA). THOMAS, Megan [CA/CA]; 5100 Spectrum A61K 31/197 (2006.01) A61K 33/42 (2006.01) Way, Mississauga, Ontario L4W 5S2 (CA). A61K 31/185 (2006.01) A61K 36/18 (2006.01) A61K 31/7004 (2006.01) (74) Agent: Torys LLP; 3000-79 Wellington Street West, Box 270, TD Centre, Toronto, Ontario M5K 1N2 (CA). (21) International Application Number: (81) Designated States (unless otherwise indicated, for every PCT/CA2006/001512 kind of national protection available): AE, AG, AL, AM, AT,AU, AZ, BA, BB, BG, BR, BW, BY, BZ, CA, CH, CN, (22) International Filing Date: CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, EG, ES, FI, 14 September 2006 (14.09.2006) GB, GD, GE, GH, GM, HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LT, (25) Filing Language: English LU, LV,LY,MA, MD, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PG, PH, PL, PT, RO, RS, RU, (26) Publication Language: English SC, SD, SE, SG, SK, SL, SM, SV, SY, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW (30) Priority Data: 60/776,325 23 February 2006 (23.02.2006) US (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant (for all designated States except US): NEW GM, KE, LS, MW, MZ, NA, SD, SL, SZ, TZ, UG, ZM, CELL FORMULATIONS LTD. -
Adjunctive Care for Lyme Disease and Co-Infections: a Naturopathic Perspective By: Dr
Adjunctive Care for Lyme Disease and Co-infections: A Naturopathic Perspective By: Dr. Deborah Sellars, N.D. www.naturofm.com 1) Common Obstacles to Curing Lyme Disease a) Immune, Endocrine, Blood Sugar and Neurotransmitter imbalances b) Gastrointestinal Disorders: i) Candida and over growth of other pathogenic yeast, parasites and bacteria. ii) Leaky Gut: Permeability of the intestines associated with Food sensitivities iii) (primarily gluten and dairy, however a food intolerance assessment may need to be done). iv) Just plain poor food choices c) Biofilms: a fibrin and plasmin coating created so that parasites, bacteria and heavy metals can evade immune recognition and elimination. d) Heavy Metal Toxicity: Primarily lead and mercury. e) Environmental Toxicity f) Excessive stress g) Mold Toxicity h) Viral Infections: Cytomegalovirus (CMV), Ebstein Barr Virus (EBV) and Human herpesvirus 6 (HHV-6) i) If the aforementioned are addressed effectively the healing process , will speed up and often create a strong enough vital force so that killing off the bugs is secondary. 2) Don’t get Over-whelmed; Start with the Basics a) Support Gut function i) Healing or aggravation of disease starts the moment we put something in our mouth. ii) An improperly functioning digestive tract is often the source of many of the body's ailments. Toxins produced by improperly digested foods, overgrowth of pathogenic bacteria and yeast and the endotoxins produced as the bacteria die off will worsen gut function and make the Lyme symptoms worse. b) Determine if you have any food sensitivities and eliminate them. (1) Gluten products and Dairy are two of the most common food groups.